Nature Communications (Sep 2024)

Lethal Borna disease virus 1 infections of humans and animals – in-depth molecular epidemiology and phylogeography

  • Arnt Ebinger,
  • Pauline D. Santos,
  • Florian Pfaff,
  • Ralf Dürrwald,
  • Jolanta Kolodziejek,
  • Kore Schlottau,
  • Viktoria Ruf,
  • Friederike Liesche-Starnecker,
  • Armin Ensser,
  • Klaus Korn,
  • Reiner Ulrich,
  • Jenny Fürstenau,
  • Kaspar Matiasek,
  • Florian Hansmann,
  • Torsten Seuberlich,
  • Daniel Nobach,
  • Matthias Müller,
  • Antonie Neubauer-Juric,
  • Marcel Suchowski,
  • Markus Bauswein,
  • Hans-Helmut Niller,
  • Barbara Schmidt,
  • Dennis Tappe,
  • Daniel Cadar,
  • Timo Homeier-Bachmann,
  • Viola C. Haring,
  • Kirsten Pörtner,
  • Christina Frank,
  • Lars Mundhenk,
  • Bernd Hoffmann,
  • Jochen Herms,
  • Wolfgang Baumgärtner,
  • Norbert Nowotny,
  • Jürgen Schlegel,
  • Rainer G. Ulrich,
  • Martin Beer,
  • Dennis Rubbenstroth

DOI
https://doi.org/10.1038/s41467-024-52192-x
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 16

Abstract

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Abstract Borna disease virus 1 (BoDV-1) is the causative agent of Borna disease, a fatal neurologic disorder of domestic mammals and humans, resulting from spill-over infection from its natural reservoir host, the bicolored white-toothed shrew (Crocidura leucodon). The known BoDV-1-endemic area is remarkably restricted to parts of Germany, Austria, Switzerland and Liechtenstein. To gain comprehensive data on its occurrence, we analysed diagnostic material from suspected BoDV-1-induced encephalitis cases based on clinical and/or histopathological diagnosis. BoDV-1 infection was confirmed by RT-qPCR in 207 domestic mammals, 28 humans and seven wild shrews. Thereby, this study markedly raises the number of published laboratory-confirmed human BoDV-1 infections and provides a first comprehensive summary. Generation of 136 new BoDV-1 genome sequences from animals and humans facilitated an in-depth phylogeographic analysis, allowing for the definition of risk areas for zoonotic BoDV-1 transmission and facilitating the assessment of geographical infection sources. Consistent with the low mobility of its reservoir host, BoDV-1 sequences showed a remarkable geographic association, with individual phylogenetic clades occupying distinct areas. The closest genetic relatives of most human-derived BoDV-1 sequences were located at distances of less than 40 km, indicating that spill-over transmission from the natural reservoir usually occurs in the patient´s home region.